首页> 美国卫生研究院文献>other >Expression of dehydratase domains from a polyunsaturated fatty acid synthase increases the production of fatty acids in Escherichia coli
【2h】

Expression of dehydratase domains from a polyunsaturated fatty acid synthase increases the production of fatty acids in Escherichia coli

机译:从多不饱和脂肪酸合酶表达脱水酶结构域可增加大肠杆菌中脂肪酸的产生

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Increasing the production of fatty acids by microbial fermentation remains an important step towards the generation of biodiesel and other portable liquid fuels. In this work, we report an Escherichia coli strain engineered to overexpress a fragment consisting of four dehydratase domains from the polyunsaturated fatty acid (PUFA) synthase enzyme complex from the deep-sea bacterium, Photobacterium profundum. The DH1-DH2-UMA enzyme fragment was excised from its natural context within a multi-enzyme PKS and expressed as a stand-alone protein. Fatty acids were extracted from the cell pellet, esterified with methanol and quantified by GC-MS analysis. Results show that the E. coli strain expressing the DH tetradomain fragment was capable of producing up to a 5-fold increase (80.31 mg total FA/L culture) in total fatty acids over the negative control strain lacking the recombinant enzyme. The enhancement in production was observed across the board for all the fatty acids that are typically made by E. coli. The overexpression of the DH tetradomain did not affect E. coli cell growth, thus showing that the observed enhancement in fatty acid production was not a result of effects associated with cell density. The observed enhancement was more pronounced at lower temperatures (3.8-fold at 16 °C, 3.5-fold at 22 °C and 1.5-fold at 30 °C) and supplementation of the media with 0.4% glycerol did not result in an increase in fatty acid production. All these results taken together suggest that either the dehydration of fatty acid intermediates are a limiting step in the E. coli fatty acid biosynthesis machinery, or that the recombinant dehydratase domains used in this study are also capable of catalyzing thioester hydrolysis of the final products. The enzyme in this report is a new tool which could be incorporated into other existing strategies aimed at improving fatty acid production in bacterial fermentations towards accessible biodiesel precursors.
机译:通过微生物发酵增加脂肪酸的产量仍然是生物柴油和其他便携式液体燃料生产的重要一步。在这项工作中,我们报告了一种大肠杆菌菌株,该菌株经过工程改造,可以过表达由深海细菌深部细菌杆菌(Photobacter profundum)的多不饱和脂肪酸(PUFA)合酶复合物组成的四个脱水酶结构域组成的片段。 DH1-DH2-UMA酶片段在多酶PKS中从其自然环境中切除,并表达为独立的蛋白质。从细胞沉淀物中提取脂肪酸,用甲醇酯化并通过GC-MS分析定量。结果表明,表达DH四结构域片段的大肠杆菌菌株与不含重组酶的阴性对照菌株相比,总脂肪酸最多可产生5倍的增加(总FA / L培养物为80.31 mg)。对于大肠杆菌通常制造的所有脂肪酸,全线观察到了产量的提高。 DH四结构域的过表达不影响大肠杆菌细胞的生长,因此表明所观察到的脂肪酸生产增强不是与细胞密度相关的结果。在较低的温度下(在16°C时为3.8倍,在22°C时为3.5倍,在30°C时为1.5倍),观察到的增强作用更为明显,向培养基中添加0.4%甘油不会增加脂肪酸生产。所有这些结果加在一起表明,脂肪酸中间体的脱水是大肠杆菌脂肪酸生物合成机制中的一个限制步骤,或者该研究中使用的重组脱水酶结构域也能够催化最终产物的硫酯水解。本报告中的酶是一种新工具,可以与其他现有策略结合使用,这些策略旨在提高细菌发酵过程中向可利用的生物柴油前体的脂肪酸产生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号